Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sensititre , Ltd. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K960220 | SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES | Sensititre , Ltd. | 1996-03-11 | 55 | 0 |
| K911419 | SENSITITRE ARIS MODULE | Sensititre , Ltd. | 1992-07-01 | 457 | 0 |
| K880641 | SENSITITRE STABILITY PLATES | Sensititre , Ltd. | 1988-05-13 | 92 | 9 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda